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  2. Alkene - Wikipedia

    en.wikipedia.org/wiki/Alkene

    Alkenes react with percarboxylic acids and even hydrogen peroxide to yield epoxides: RCH=CH 2 + RCO 3 H → RCHOCH 2 + RCO 2 H. For ethylene, the epoxidation is conducted on a very large scale industrially using oxygen in the presence of silver-based catalysts: C 2 H 4 + 1/ 2 O 2 → C 2 H 4 O. Alkenes react with ozone, leading to the scission ...

  3. Category:Alkenes - Wikipedia

    en.wikipedia.org/wiki/Category:Alkenes

    Alkenes are hydrocarbons that have one or more double bonds between carbon atoms. Subcategories. This category has the following 11 subcategories, out of 11 total. A.

  4. Hydroboration - Wikipedia

    en.wikipedia.org/wiki/Hydroboration

    Hydroboration of 1,2-disubstituted alkenes, such as a cis or trans olefin, produces generally a mixture of the two organoboranes of comparable amounts, even if the steric properties of the substituents are very different. For such 1,2-disubstituted olefins, regioselectivity can be observed only when one of the two substituents is a phenyl ring.

  5. Alken - Wikipedia

    en.wikipedia.org/wiki/Alken

    Alkene[s], unsaturated hydrocarbons that contain at least one carbon-carbon double bond This page was last edited on 31 October 2022, at 17:57 (UTC). Text is ...

  6. Decene - Wikipedia

    en.wikipedia.org/wiki/Decene

    Decene / d ɛ k iː n / is an organic compound with the chemical formula C 10 H 20.Decene contains a chain of ten carbon atoms with one double bond, making it an alkene.There are many isomers of decene depending on the position and geometry of the double bond.

  7. C5H10 - Wikipedia

    en.wikipedia.org/wiki/C5H10

    This page was last edited on 24 October 2023, at 07:57 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  8. Terminal alkene - Wikipedia

    en.wikipedia.org/wiki/Terminal_alkene

    There are two types of alpha-olefins, branched and linear (or normal). The chemical properties of branched alpha-olefins with a branch at either the second (vinylidene) or the third carbon number are significantly different from the properties of linear alpha-olefins and those with branches on the fourth carbon number and further from the start of the chain.

  9. Dehydrogenation - Wikipedia

    en.wikipedia.org/wiki/Dehydrogenation

    Alkenes are precursors to aldehydes (R−CH=O), alcohols (R−OH), polymers, and aromatics. [1] As a problematic reaction, the fouling and inactivation of many catalysts arises via coking, which is the dehydrogenative polymerization of organic substrates. [2] Enzymes that catalyze dehydrogenation are called dehydrogenases.